A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580241



Internal ID16367650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54632002..54671963hg38UCSC Ensembl
Innerchr19:55143452..55183414hg19UCSC Ensembl
Innerchr19:59835264..59875226hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3839962
hg1939963
hg1839963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901637
Samples
Known GenesLILRB1, LILRB4, MIR8061
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580241
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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